US4190434A - Thermal processes for the production of magnesium - Google Patents
Thermal processes for the production of magnesium Download PDFInfo
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- US4190434A US4190434A US05/915,387 US91538778A US4190434A US 4190434 A US4190434 A US 4190434A US 91538778 A US91538778 A US 91538778A US 4190434 A US4190434 A US 4190434A
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- magnesium
- slag
- aluminum
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- sio
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- 239000011777 magnesium Substances 0.000 title claims abstract description 25
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 title claims abstract description 23
- 229910052749 magnesium Inorganic materials 0.000 title claims abstract description 22
- 238000000034 method Methods 0.000 title claims abstract description 19
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 13
- 239000002893 slag Substances 0.000 claims abstract description 36
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims abstract description 31
- 239000000395 magnesium oxide Substances 0.000 claims abstract description 30
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 22
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims abstract description 19
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 15
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000011651 chromium Substances 0.000 claims abstract description 6
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 29
- 239000000377 silicon dioxide Substances 0.000 claims description 14
- 229910052681 coesite Inorganic materials 0.000 claims description 13
- 229910052906 cristobalite Inorganic materials 0.000 claims description 13
- 229910052682 stishovite Inorganic materials 0.000 claims description 13
- 229910052905 tridymite Inorganic materials 0.000 claims description 13
- 229910018404 Al2 O3 Inorganic materials 0.000 claims description 11
- 229910000604 Ferrochrome Inorganic materials 0.000 claims description 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 7
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims description 4
- 235000011941 Tilia x europaea Nutrition 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 claims description 4
- 238000009833 condensation Methods 0.000 claims description 4
- 230000005494 condensation Effects 0.000 claims description 4
- 239000004571 lime Substances 0.000 claims description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 3
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- 238000004064 recycling Methods 0.000 claims 1
- 239000010459 dolomite Substances 0.000 abstract description 10
- 229910000514 dolomite Inorganic materials 0.000 abstract description 10
- 229910052710 silicon Inorganic materials 0.000 abstract description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 5
- 239000010703 silicon Substances 0.000 abstract description 5
- 229910045601 alloy Inorganic materials 0.000 abstract description 4
- 239000000956 alloy Substances 0.000 abstract description 4
- 229910052799 carbon Inorganic materials 0.000 abstract description 4
- 235000000396 iron Nutrition 0.000 abstract 1
- 238000011084 recovery Methods 0.000 abstract 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 29
- 239000000203 mixture Substances 0.000 description 19
- 229910052742 iron Inorganic materials 0.000 description 14
- 229910001570 bauxite Inorganic materials 0.000 description 10
- 239000007788 liquid Substances 0.000 description 7
- 229910000519 Ferrosilicon Inorganic materials 0.000 description 6
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
- 238000007792 addition Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
- 229910019830 Cr2 O3 Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229910005347 FeSi Inorganic materials 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B26/00—Obtaining alkali, alkaline earth metals or magnesium
- C22B26/20—Obtaining alkaline earth metals or magnesium
- C22B26/22—Obtaining magnesium
Definitions
- the present invention relates to improvements to thermal processes for the production of magnesium.
- magnesium by the reduction of substances containing magnesium oxide, using various reducing agents such as silicon, aluminum or calcium, either separately or as mixtures, or alloys with each other, or with other elements such as iron.
- the MAGNETHERM process which is the best known of these processes, described in French Pat. No. 1,194,556, enables magnesium to be obtained by reduction at a high temperature of a substance containing magnesium oxide by means of a reducing agent whose products of oxidation are not gaseous at the reaction temperature, the said substance which contains magnesium oxide and the said reducing agent being delivered to the surface of a bath of slag kept liquid by an electric current at a pressure above 1.8 millibars so that the magnesium vapors obtained are condensed in the liquid state.
- FIG. 1. is a schemitic representation reduced to the essential elements of a type of furnace for carrying out the MAGNETHERM process.
- FIGS. 2 and 3 are diagrammatic representations of the preferential ferro-silico-chrome slags and ferro-silico-aluminum reducing agents of the instant invention.
- (1) is the carbon lining covering the side walls; (2) is the refractory and heat insulating lining; (3) is the impervious outer body made of steel plates; (4) is the carbon base, and (5) is the current output; (6) is the tap hole for periodic removal of the residual ferro-silicon which has only a low silicon content and of the excess liquid slag. This tap hole is tightly closed when the furnace is in operation.
- the dome of the furnace has a non-conducting and heat insulating lining (7).
- the wide opening (8) constitutes the tuyere which enables the magnesium vapors to flow towards the condensation chamber.
- the axial pipe (9) accommodates the vertical electrode (10) consisting of a graphite sleeve (11) which is permanently immersed in the liquid slag and attached to the lower end of a copper tube through which water circulates.
- An inlet pipe (12) is provided for the introduction of the reactants.
- (13--13) indicates the maximum upper level of the liquid slag and (14--14) indicates the minimum lower level.
- the condensation chamber consists of two main parts, namely, the condenser, properly speaking, and the crucible for reception of the magnesium.
- the condenser (15) has a refractory lining (16) and a vacuum tight steel plating forming the external wall.
- the inlet pipe (17) for vacuum pumps is mounted at the top and forms the upper covering to the condenser.
- the condenser is connected to the furnace by the flange connection (18) which is adapted to be cooled by circulating water as are also all the other clamps of the furnace.
- Thermo-electric couples are provided to measure the temperature at various points and temperature controls enable the various temperatures to be maintained at their predetermined values.
- the magnesium produced is conducted as a vapor to the condenser (15) which is designed to condense the magnesium to a liquid which trickles down and collects in the crucible (19) where it may either be kept in the liquid state or solidified by cooling.
- the optimum condensation yield is obtained in this way.
- the electric power is provided by an auto transformer in which the voltage can be varied continuously (or discontinuously with only very slight intervals). This arrangement is essential to enable the power output of the furnace to be controlled from moment to moment and hence also the course of the reaction by which the magnesium is produced.
- the process is carried out at a temperature of ca. 1550 to 1600° C. under a pressure of from 27 to 47 millibars and the magnesium is extracted with an extraction yield of at least 85%.
- the Mg content of the magnesium metal obtained is at least 99.60% and may be as high as 99.90%.
- the residual ferrosilicon contains less than 20% of Si.
- the magnesium oxide used for the MAGNETHERM process may be obtained from various sources, such, for example, as from sea water or from calcined dolomite in which the lime contributes to the formation of the slag.
- magnesium from various sources may be used.
- the applicant has found that it is particularly advantageous to use, as source of magnesium oxide, waste products containing at least 20%, preferably at least 30% of MgO and at least 20%, preferably at least 25% of Al 2 O 3 , particularly slag left from the production of chrome iron, in particular carbon-containing chrome iron from certain types of ores which contain a high proportion of magnesium oxide.
- composition of these slags may vary within the following approximate limits (in percent by weight):
- a high quality calcined dolomite has a composition within the following approximate limits:
- the magnesium oxide content of the chrome iron slags is thus only slightly lower and some times even equal to that of calcined dolomite.
- the lime content is relatively low while the alumina content is much higher. This last factor is an advantage.
- the molecular ratio of CaO to SiO 2 should be at least equal to 1.8 and preferably from 2.2 to 2.4, the molecular ratio of Al 2 O 3 to SiO 2 should be at least equal to 0.26 and preferably from 0.30 to 0.33 and the MgO content should be between 3 and 8%.
- composition of the slag should be within the following limits:
- the melting point is in the range of from 1500° to 1700° C.
- the introduction into a furnace of chrome iron slag as source of magnesium oxide therefore requires a correction of the composition by various additions to maintain the composition of the slag within the limits indicated above.
- the composition of the reducing agent may be modified and a ferro-silico-aluminum may be used.
- bauxite which entails considerable difficulties since it must be used in a relatively pure state with a low iron oxide content, may thereby be reduced and even completely eliminated.
- the content of silicon and aluminum in the ferro-silico-aluminum used as reducing agent should be calculated according to the composition of the chrome iron slag used and the qunatity introduced into the furnace so that the composition of the slag will be maintained within the limits indicated above.
- FIGS. 2 and 3 indicate the shaded zones, the preferential compositions of ferro-silico-chrome slags (considering only the total Si0 2 +Mg0+Al 2 0 3 content) and of the ferro-silico-aluminum reducing agent.
- ferro-silico-aluminum as reducing agent, three tests were carried out using, as reducing agent, respectively, a 75% ferro-silicon with the addition of bauxite, and a ferro-silico-aluminum containing 8.60% of aluminum with the addition of bauxite and the same ferro-silica-aluminum without the additon of bauxite.
- Example 2 shows that if an 8.6% ferro-silico-aluminum is used, good results can be obtained only if bauxite is added in an amount substantially equal in weight to the chrome iron slag.
- Example 3 shows that very poor results are obtained if bauxite is omitted because the composition of the slag is then imbalanced and no longer conforms to the optimum conditions for the reduction of magnesium oxide.
- the FeCr had the following composition:
- ferro-silico-aluminum had the following composition:
- chrome iron slags as source of magnesium has various advantages. This substance is completely dehydrated and has no tendency to take up water. There is therefore no need to calcine it before use as in the case of dolomite. Its storage even for prolonged periods requires no special precautions.
- a charge according to this invention is calculated on the following basis:
- the amount of Mg theoretically produced is 259 kg (100% yield), which is 16.1% more than in the first case.
- the weight of the charge is greater by 2.7% but the volume is slightly less due to the higher density of chrome iron slag.
- An additional advantage of the process of this invention lies in the fact that the chromium initially contained in the chrome iron slag, either in the form of chromium oxide or in the form of metallic inclusions of chrome iron, passes virtually completely into the residual ferro-silicon which is collected at the end of each operation.
- the residual alloy had a composition varying within the following limits:
- This ferro-silicon-chrome residual alloy may be reintroduced into certain operating cycles for the production of ferrochrome or crude chromium.
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- Environmental & Geological Engineering (AREA)
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- Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- Organic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
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Abstract
This invention relates to the thermal production of magnesium, using, as source of magnesium oxide, a residual slag from the manufacture of certain carbon-containing chrome irons and, as reducing agent, a ferro-silico-aluminum for carrying out the MAGNETHERM process. Magnesium is obtained with a high degree of purity and in excellent yields, with the recovery of a residual alloy containing chromium and silicon, and the production capacity of a given furnace is increased by about 16% compared with that obtained when using calcined dolomite.
Description
The present invention relates to improvements to thermal processes for the production of magnesium.
It is known to produce magnesium by the reduction of substances containing magnesium oxide, using various reducing agents such as silicon, aluminum or calcium, either separately or as mixtures, or alloys with each other, or with other elements such as iron.
The MAGNETHERM process, which is the best known of these processes, described in French Pat. No. 1,194,556, enables magnesium to be obtained by reduction at a high temperature of a substance containing magnesium oxide by means of a reducing agent whose products of oxidation are not gaseous at the reaction temperature, the said substance which contains magnesium oxide and the said reducing agent being delivered to the surface of a bath of slag kept liquid by an electric current at a pressure above 1.8 millibars so that the magnesium vapors obtained are condensed in the liquid state.
FIG. 1. is a schemitic representation reduced to the essential elements of a type of furnace for carrying out the MAGNETHERM process.
FIGS. 2 and 3 are diagrammatic representations of the preferential ferro-silico-chrome slags and ferro-silico-aluminum reducing agents of the instant invention.
With respect to FIG. 1, (1) is the carbon lining covering the side walls; (2) is the refractory and heat insulating lining; (3) is the impervious outer body made of steel plates; (4) is the carbon base, and (5) is the current output; (6) is the tap hole for periodic removal of the residual ferro-silicon which has only a low silicon content and of the excess liquid slag. This tap hole is tightly closed when the furnace is in operation.
The dome of the furnace has a non-conducting and heat insulating lining (7). The wide opening (8) constitutes the tuyere which enables the magnesium vapors to flow towards the condensation chamber. The axial pipe (9) accommodates the vertical electrode (10) consisting of a graphite sleeve (11) which is permanently immersed in the liquid slag and attached to the lower end of a copper tube through which water circulates. An inlet pipe (12) is provided for the introduction of the reactants. (13--13) indicates the maximum upper level of the liquid slag and (14--14) indicates the minimum lower level.
The condensation chamber consists of two main parts, namely, the condenser, properly speaking, and the crucible for reception of the magnesium.
The condenser (15) has a refractory lining (16) and a vacuum tight steel plating forming the external wall. The inlet pipe (17) for vacuum pumps is mounted at the top and forms the upper covering to the condenser.
The condenser is connected to the furnace by the flange connection (18) which is adapted to be cooled by circulating water as are also all the other clamps of the furnace.
Thermo-electric couples are provided to measure the temperature at various points and temperature controls enable the various temperatures to be maintained at their predetermined values.
The magnesium produced is conducted as a vapor to the condenser (15) which is designed to condense the magnesium to a liquid which trickles down and collects in the crucible (19) where it may either be kept in the liquid state or solidified by cooling. The optimum condensation yield is obtained in this way.
The electric power is provided by an auto transformer in which the voltage can be varied continuously (or discontinuously with only very slight intervals). This arrangement is essential to enable the power output of the furnace to be controlled from moment to moment and hence also the course of the reaction by which the magnesium is produced.
The following is given as an example. A slag having the following composition:
Ca O: 54.90%
SiO2 : 24.60%
Al2 O3 :13.40%
MgO : 6.60%
is used with a reducing agent consisting of ferrosilicon particles containing 75% Si and measuring 0 to 30 mm and a calcined dolomite containing 37% of MgO and measuring 3/30 mm before heat treatment. The process is carried out at a temperature of ca. 1550 to 1600° C. under a pressure of from 27 to 47 millibars and the magnesium is extracted with an extraction yield of at least 85%. The Mg content of the magnesium metal obtained is at least 99.60% and may be as high as 99.90%.
The residual ferrosilicon contains less than 20% of Si.
The magnesium oxide used for the MAGNETHERM process may be obtained from various sources, such, for example, as from sea water or from calcined dolomite in which the lime contributes to the formation of the slag.
In view of the flexibility of this process, magnesium from various sources may be used. The applicant has found that it is particularly advantageous to use, as source of magnesium oxide, waste products containing at least 20%, preferably at least 30% of MgO and at least 20%, preferably at least 25% of Al2 O3, particularly slag left from the production of chrome iron, in particular carbon-containing chrome iron from certain types of ores which contain a high proportion of magnesium oxide.
Depending on the geographical source of the ores and the process employed for production of the chrome iron, the composition of these slags may vary within the following approximate limits (in percent by weight):
MgO: 20-40%
Al2 O3 :20-35%
SiO2 :20-35%
CaO:<10%
Cr2 O3 :<10%
TiO2 :<1%
FeO:<5%
MnO:approx 0.15%
By comparison, a high quality calcined dolomite has a composition within the following approximate limits:
MgO:35-43%
SiO2 :1-2%
Al2 O3 :<1%
CaO:63-57%
The magnesium oxide content of the chrome iron slags is thus only slightly lower and some times even equal to that of calcined dolomite. The lime content, on the other hand, is relatively low while the alumina content is much higher. This last factor is an advantage.
It is known that, for obtaining optimum yields from the MAGNETHERM process, it is necessary to use a composition of slag within certain limits which determine both its melting point and its physico-chemical activity.
In particular, the molecular ratio of CaO to SiO2 should be at least equal to 1.8 and preferably from 2.2 to 2.4, the molecular ratio of Al2 O3 to SiO2 should be at least equal to 0.26 and preferably from 0.30 to 0.33 and the MgO content should be between 3 and 8%.
The composition of the slag should be within the following limits:
CaO:54-58%
SiO:23-28%
Al2 O3 :11-15%
MgO:3-8.50%
Under these conditions, the melting point is in the range of from 1500° to 1700° C. The introduction into a furnace of chrome iron slag as source of magnesium oxide therefore requires a correction of the composition by various additions to maintain the composition of the slag within the limits indicated above. Furthermore, and this is also an object of the present invention, the composition of the reducing agent may be modified and a ferro-silico-aluminum may be used. The use of bauxite, which entails considerable difficulties since it must be used in a relatively pure state with a low iron oxide content, may thereby be reduced and even completely eliminated.
It has been found, in practice, that the most favorable composition of chrome iron slags is within the following limits, calculated in relation to the total (SiO2 +MgO+Al2 O3):
MgO:≧30%
Al2 O3 :≧25 %
SiO2 :≧35%
The content of silicon and aluminum in the ferro-silico-aluminum used as reducing agent should be calculated according to the composition of the chrome iron slag used and the qunatity introduced into the furnace so that the composition of the slag will be maintained within the limits indicated above.
The triangular diagrams of FIGS. 2 and 3 indicate the shaded zones, the preferential compositions of ferro-silico-chrome slags (considering only the total Si02 +Mg0+Al2 03 content) and of the ferro-silico-aluminum reducing agent.
To demonstrate the significance and difficulty of using ferro-silico-aluminum as reducing agent, three tests were carried out using, as reducing agent, respectively, a 75% ferro-silicon with the addition of bauxite, and a ferro-silico-aluminum containing 8.60% of aluminum with the addition of bauxite and the same ferro-silica-aluminum without the additon of bauxite.
All three tests were carried out in a MAGNETHERM furnace of 2,000 KVA, using a chrome iron slag having the following composition:
MgO:36%
SiO2 :28%
Al2 O3 :27%
Cr2 O3 :3.20%
FeO:1.60%
CaO:2%
MnO:0.15%
TiO2 :0.35%
The data obtained from the three tests are summarized in the following table:
______________________________________
Example 1
Example 2 Example 3
______________________________________
Calcined dolomite
21,600 kg 21,600 kg 18,700 kg
FeCr slag 1,545 kg 1,998 kg 6,545 kg
Bauxite containing
74% Al.sub.2 O.sub.3
2,868 kg 1,998 kg --
Reducing
nature FeSi 75%
FeSiAl 8.6
FeSiAl 8.6%
agent Si Al Al
66.0% Si
66.0% Si
weight 3,824 kg
4,168 kg
4,675 kg
Si content of residual
FeSi 20% 20% 28%
Magnesium obtained as
ingot after refining
3,500 kg 3,660 kg 1,760 kg
______________________________________
Example 2 shows that if an 8.6% ferro-silico-aluminum is used, good results can be obtained only if bauxite is added in an amount substantially equal in weight to the chrome iron slag.
Example 3 shows that very poor results are obtained if bauxite is omitted because the composition of the slag is then imbalanced and no longer conforms to the optimum conditions for the reduction of magnesium oxide.
Into a MAGNETHERM furnace identical in construction to that described above, but with a power of 4,500 KVA, initially containing ca. 18 tons of molten slag having the following composition:
______________________________________
SiO.sub.2 25.40%
Al.sub.2 O.sub.3
12.20%
CaO 56.70%
MgO 5.40%
Molecular CaO/SiO.sub.2 2.39%
ratios Al.sub.2 O.sub.3 /SiO.sub.2
0.28%
______________________________________
there were introduced:
Calcined dolomite containing 36.8% MgO:42,596 kg
FeCr slag:7,266 kg
FeSiAl containing 20% Al:8,114 kg
Energy consumption:72.l MWh.
The FeCr had the following composition:
SiO2 :26.00%
Al2 O3 :27.00%
MgO:34.00%
Cr2 O3 :10.00%
FeO :1.60%
CaO:2.50%
MnO:0.15%
TiO2 :0.70%
and the ferro-silico-aluminum had the following composition:
Al:19.00 l% Si:65.70%
and the residual metal was found to contain 20% of silicon.
This operation, which lasted 15 hours, yielded 8,930 kg of magnesium ingot after refining.
This example demonstrates that if a ferro-silico-aluminum containing 20% of aluminum is used as reducing agent, the addition of bauxite can be completely omitted and yet the same yields and same quality of magnesium can be maintained. An aluminum content of between 15 and 25% provides satisfactory results in practice. Beyond this amount, there would be an excess of aluminum oxide in the slag, which would have to be compensated.
The use of chrome iron slags as source of magnesium has various advantages. This substance is completely dehydrated and has no tendency to take up water. There is therefore no need to calcine it before use as in the case of dolomite. Its storage even for prolonged periods requires no special precautions.
Its aluminum oxide content permits the addition of bauxite to be ommitted. This is an economical advantage as well as enabling the weight of the furnace charge (and hence also the volume) to be reduced by about 16% for the production of an equal amount of magnesium or, alternatively, the production capacity of a given furnace can be increased by 16% for an equal charge.
A normal "MAGNETHERM" charge is in fact calculated on the basis of
______________________________________ 1,000 kg of calcined dolomite (370 kg MgO) 140 kg of calcined bauxite (105 kg Al.sub.2 O.sub.3) 175 kg of 75% ferro-silicon 1,315 kg ______________________________________
This theoretically produces 223 kg of Mg (100% yield).
A charge according to this invention is calculated on the following basis:
______________________________________
1,000 kg of calcined dolomite (370 kg MgO)
170 kg of FeCr slag
59 kg MgO
46 kg Al.sub.2 O.sub.3
180 kg of FeSiAl 20% Al
68% Si
1,350 kg
______________________________________
The amount of Mg theoretically produced is 259 kg (100% yield), which is 16.1% more than in the first case. The weight of the charge is greater by 2.7% but the volume is slightly less due to the higher density of chrome iron slag.
An additional advantage of the process of this invention lies in the fact that the chromium initially contained in the chrome iron slag, either in the form of chromium oxide or in the form of metallic inclusions of chrome iron, passes virtually completely into the residual ferro-silicon which is collected at the end of each operation.
In the various operations which have been described, the residual alloy had a composition varying within the following limits:
Si:22.50-19.50%
Fe:60.00-58.00%
Al:0.16-0.17%
Cu:0.14-0.17%
Ti:1.20-1.70%
Mn:0.40-0.50%
Ca:0.13-0.07%
Cr:14.20-16.20%
This ferro-silicon-chrome residual alloy may be reintroduced into certain operating cycles for the production of ferrochrome or crude chromium.
Claims (7)
1. A thermal process for the production of magnesium in a closed electric furnace in which magnesium oxide and a metallic reducing agent react in the presence of a molten slag to produce magnesium vapors which are transmitted from the reaction furnace to a condensation zone wherein the vapors are condensed to magnesium, the improvement wherein at least a part of the magnesium oxide is introduced into the furnace in the form of a slag from the manufacture of ferro-chromium and which contains at least 20% by weight magnesium oxide and at least 25% by weight aluminum oxide, and in which the molten slag is formed essentially of lime, silica and alumina present in the molecular ratio of CaO/SiO2 of at least 1.8 and Al2 O3 /SiO2 of at least 0.26.
2. A process as claimed in claim 1 in which the lime, silica and alumina are present in the molten slag in the molecular ratio of CaO/SiO2 within the range of 2.2-2.4 and Al2 O3 /SiO2 are present within the range of 0.3-0.33.
3. The process as claimed in claim 1 in which the metallic reducing agent is a ferro-silico-aluminum metal containing more than 8% by weight of aluminum.
4. A process as claimed in claim 3 in which the ferro-silico-aluminum contains 15-25% by weight of aluminum.
5. A process as claimed in claim 1 which includes the additional step of reclaiming the metallic reducing agent as a residual containing chromium and recycling said residual metal for the production of ferro-chromium or crude chromium.
6. The process as claimed in claim 1 which includes maintaining the slag at a temperature within the range of 1500-1700° C. during the reaction for reducing the magnesium oxide in the slag.
7. The method as claimed in claim 1 which includes the step of maintaining the pressure in the closed electric furnace within the range of 27-47 millibars.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7720227A FR2395319A1 (en) | 1977-06-24 | 1977-06-24 | IMPROVEMENTS IN THERMAL MAGNESIUM PRODUCTION PROCESSES |
| FR7720227 | 1977-06-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4190434A true US4190434A (en) | 1980-02-26 |
Family
ID=9192821
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US05/915,387 Expired - Lifetime US4190434A (en) | 1977-06-24 | 1978-06-14 | Thermal processes for the production of magnesium |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US4190434A (en) |
| JP (1) | JPS5410213A (en) |
| BR (1) | BR7803968A (en) |
| CA (1) | CA1108409A (en) |
| ES (1) | ES470960A1 (en) |
| FR (1) | FR2395319A1 (en) |
| GR (1) | GR62268B (en) |
| IN (1) | IN147742B (en) |
| IT (1) | IT1096555B (en) |
| NO (1) | NO154729C (en) |
| OA (1) | OA08230A (en) |
| TR (1) | TR19951A (en) |
| YU (1) | YU146478A (en) |
| ZA (1) | ZA783582B (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4364771A (en) * | 1979-05-15 | 1982-12-21 | Societe Francaise D'electrometallurgie Sofrem | Product for the desulphurization of cast irons and steels |
| US4478637A (en) * | 1983-03-10 | 1984-10-23 | Aluminum Company Of America | Thermal reduction process for production of magnesium |
| US4543122A (en) * | 1983-10-19 | 1985-09-24 | Johannesburg Consolidated Investment Company Limited | Magnesium production |
| US4572736A (en) * | 1983-12-21 | 1986-02-25 | Shell Internationale Research Maatschappij B.V. | Process for producing magnesium |
| WO1989000613A1 (en) * | 1987-07-10 | 1989-01-26 | The University Of Manchester Institute Of Science | Magnesium production |
| US5383953A (en) * | 1994-02-03 | 1995-01-24 | Aluminum Company Of America | Method of producing magnesium vapor at atmospheric pressure |
| US6179897B1 (en) | 1999-03-18 | 2001-01-30 | Brookhaven Science Associates | Method for the generation of variable density metal vapors which bypasses the liquidus phase |
| US8617457B2 (en) | 2011-07-08 | 2013-12-31 | Infinium, Inc. | Apparatus and method for condensing metal vapor |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2463190B1 (en) * | 1979-08-08 | 1985-11-08 | Vasipari Kutato Intezet | METALLOTHERMAL PROCESS FOR THE SIMULTANEOUS PRODUCTION OF MAGNESIUM AND CEMENT OR CALCIUM AND CEMENT |
| US4582532A (en) * | 1985-05-02 | 1986-04-15 | Aluminum Company Of America | Thermal reduction process for production of calcium using aluminum as a reductant |
| KR101325532B1 (en) * | 2012-04-27 | 2013-11-07 | 강원섭 | Ferro-silicon and magnesium production methods using ferro-nickel slag, and production apparatus and melting reduction furnace therefor |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1194556A (en) | 1958-04-09 | 1959-11-10 | Le Magnesium Thermique | Magnesium manufacturing process |
| US2971833A (en) * | 1958-04-09 | 1961-02-14 | Le Magnesium Thermique Soc | Process of manufacturing magnesium |
| US3658509A (en) * | 1969-02-03 | 1972-04-25 | Julian M Avery | Process for the metallothermic production of magnesium |
| US3681053A (en) * | 1970-04-06 | 1972-08-01 | Julian M Avery | Use of high-silicon as the reductant for the metallothermic production of magnesium |
| US3698888A (en) * | 1970-04-06 | 1972-10-17 | Julian Miles Avery | Metallothermic production of magnesium |
| US3994717A (en) * | 1970-04-06 | 1976-11-30 | Julian Avery | Metallothermic production of magnesium in the presence of a substantially static atmosphere of inert gas |
| US4033759A (en) * | 1975-09-04 | 1977-07-05 | Ethyl Corporation | Process for producing magnesium utilizing aluminum metal reductant |
| US4033758A (en) * | 1975-09-04 | 1977-07-05 | Ethyl Corporation | Process for producing magnesium utilizing aluminum-silicon alloy reductant |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA994108A (en) * | 1972-04-18 | 1976-08-03 | Julian M. Avery | Aluminothermic production of magnesium and an oxidic slag containing recoverable alumina |
| FR2204697B1 (en) * | 1972-10-30 | 1975-01-03 | Metaux Speciaux Sa |
-
1977
- 1977-06-24 FR FR7720227A patent/FR2395319A1/en active Granted
-
1978
- 1978-05-24 IN IN390/DEL/78A patent/IN147742B/en unknown
- 1978-06-06 OA OA56522A patent/OA08230A/en unknown
- 1978-06-14 US US05/915,387 patent/US4190434A/en not_active Expired - Lifetime
- 1978-06-19 IT IT24687/78A patent/IT1096555B/en active
- 1978-06-20 GR GR56545A patent/GR62268B/en unknown
- 1978-06-20 TR TR19951A patent/TR19951A/en unknown
- 1978-06-20 ES ES470960A patent/ES470960A1/en not_active Expired
- 1978-06-20 JP JP7480878A patent/JPS5410213A/en active Pending
- 1978-06-21 YU YU01464/78A patent/YU146478A/en unknown
- 1978-06-22 BR BR787803968A patent/BR7803968A/en unknown
- 1978-06-22 NO NO782181A patent/NO154729C/en unknown
- 1978-06-22 ZA ZA00783582A patent/ZA783582B/en unknown
- 1978-06-23 CA CA306,137A patent/CA1108409A/en not_active Expired
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1194556A (en) | 1958-04-09 | 1959-11-10 | Le Magnesium Thermique | Magnesium manufacturing process |
| US2971833A (en) * | 1958-04-09 | 1961-02-14 | Le Magnesium Thermique Soc | Process of manufacturing magnesium |
| US3658509A (en) * | 1969-02-03 | 1972-04-25 | Julian M Avery | Process for the metallothermic production of magnesium |
| US3681053A (en) * | 1970-04-06 | 1972-08-01 | Julian M Avery | Use of high-silicon as the reductant for the metallothermic production of magnesium |
| US3698888A (en) * | 1970-04-06 | 1972-10-17 | Julian Miles Avery | Metallothermic production of magnesium |
| US3994717A (en) * | 1970-04-06 | 1976-11-30 | Julian Avery | Metallothermic production of magnesium in the presence of a substantially static atmosphere of inert gas |
| US4033759A (en) * | 1975-09-04 | 1977-07-05 | Ethyl Corporation | Process for producing magnesium utilizing aluminum metal reductant |
| US4033758A (en) * | 1975-09-04 | 1977-07-05 | Ethyl Corporation | Process for producing magnesium utilizing aluminum-silicon alloy reductant |
| US4066445A (en) * | 1975-09-04 | 1978-01-03 | Ethyl Corporation | Process for producing magnesium utilizing aluminum metal reductant |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4364771A (en) * | 1979-05-15 | 1982-12-21 | Societe Francaise D'electrometallurgie Sofrem | Product for the desulphurization of cast irons and steels |
| US4478637A (en) * | 1983-03-10 | 1984-10-23 | Aluminum Company Of America | Thermal reduction process for production of magnesium |
| US4543122A (en) * | 1983-10-19 | 1985-09-24 | Johannesburg Consolidated Investment Company Limited | Magnesium production |
| US4572736A (en) * | 1983-12-21 | 1986-02-25 | Shell Internationale Research Maatschappij B.V. | Process for producing magnesium |
| WO1989000613A1 (en) * | 1987-07-10 | 1989-01-26 | The University Of Manchester Institute Of Science | Magnesium production |
| US5383953A (en) * | 1994-02-03 | 1995-01-24 | Aluminum Company Of America | Method of producing magnesium vapor at atmospheric pressure |
| WO1995021274A1 (en) * | 1994-02-03 | 1995-08-10 | Aluminum Company Of America | Method of producing magnesium vapor at atmospheric pressure |
| US6179897B1 (en) | 1999-03-18 | 2001-01-30 | Brookhaven Science Associates | Method for the generation of variable density metal vapors which bypasses the liquidus phase |
| US8617457B2 (en) | 2011-07-08 | 2013-12-31 | Infinium, Inc. | Apparatus and method for condensing metal vapor |
| US8926727B2 (en) | 2011-07-08 | 2015-01-06 | Infinium, Inc. | Apparatus and method for condensing metal vapor |
Also Published As
| Publication number | Publication date |
|---|---|
| IT1096555B (en) | 1985-08-26 |
| YU146478A (en) | 1982-08-31 |
| ZA783582B (en) | 1979-07-25 |
| IN147742B (en) | 1980-06-14 |
| JPS5410213A (en) | 1979-01-25 |
| NO154729B (en) | 1986-09-01 |
| FR2395319A1 (en) | 1979-01-19 |
| NO782181L (en) | 1978-12-28 |
| CA1108409A (en) | 1981-09-08 |
| TR19951A (en) | 1980-05-16 |
| FR2395319B1 (en) | 1980-01-18 |
| ES470960A1 (en) | 1979-02-01 |
| NO154729C (en) | 1986-12-10 |
| OA08230A (en) | 1987-10-30 |
| GR62268B (en) | 1979-03-23 |
| BR7803968A (en) | 1979-01-16 |
| IT7824687A0 (en) | 1978-06-19 |
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